Senior Research Fellow - Project Toxicologist, Neuroscience and Eye Health Boehringer Ingelheim International GmbHSenior Research Fellow - Project Toxicologist, Neuroscience and Eye HealthRidgefield, CT$166,600–$250,000 / yearSupport the implementation of scientifically robust non-clinical safety strategies, spanning from NTC discovery through clinical trial execution to regulatory submission for marketing authorization, specifically for the development of intravitreal (IVT) medications in eye health across various modalities, ensuring alignment with external requirements and benchmark project strategies. Your role includes advising on all aspects of nonclinical safety for new drugs of different Modalities-covering the nonclinical testing strategy, study design, dose selection, and the overall toxicological assessments-and supporting the preparation of development plans, protocols, reports, and regulatory documents.
Building Substitute Teacher Ridgefield Public SchoolsBuilding Substitute TeacherRidgefield, CTBuilding Substitute Teacher JobID: 2318 Position Type: Substitute/Substitute TeacherDate Posted: 9/4/2026Location: Ridgebury Elementary School Additional Information: Show/HideRidgebury Elementary School has a vacancy for a Building Substitute for the 2026-27 school year. Building substitutes will be assigned any vacancy in the school that day and if no vacancy exists a principal will determine an assignment.
Postdoctoral Fellow - Clinical Development Operations Boehringer Ingelheim International GmbHPostdoctoral Fellow - Clinical Development OperationsRidgefield, CTIn collaboration with Trial Resource Specialist and with support from CRAs as appropriate, ensures collection of required documents, with timely, complete and compliant archiving of all relevant documents for the electronic Trial Master File (eTMF) and Clinical Trial Report (CTR) Appendices. The Clinical Development Operations fellowship is designed to provide the PharmD fellow with an understanding of the history of drug development and how the US Code of Federal Regulations and International Conference on Harmonization (ICH) - Good Clinical Practice (GCP) set the framework under which clinical trials are conducted.
Postdoctoral Fellow Regulatory Affairs - Chemistry, Manufacturing & Control Boehringer Ingelheim International GmbHPostdoctoral Fellow Regulatory Affairs - Chemistry, Manufacturing & ControlRidgefield, CTRegulatory Expertise: The Fellow will develop basic regulatory expertise/knowledge in one or more therapeutic areas covering multiple dosage forms while interacting effectively within Regulatory Affairs and across CMC stakeholder functions, as a regulatory advocate to achieve common goals for assigned projects. The Clinical Development and Medical Affairs Fellow is a post-doctoral pharmacist position that will obtain broad exposure to BI US Medical functions including, but not limited to -- Medical Affairs and Scientific Communications, clinical operations, translational medicine and clinical pharmacology, and regulatory affairs.
Postdoctoral Regulatory Affairs Fellow - Product Labeling Operations Boehringer Ingelheim International GmbHPostdoctoral Regulatory Affairs Fellow - Product Labeling OperationsRidgefield, CTCollaborate with Regulatory Affairs, Quality, Supply Chain, Packaging, Distribution, Global Labeling Artwork Management, and other stakeholders to support timely and compliant labeling implementation. The position offers an opportunity to be involved in critical matters related to operational labeling implementation, strategy, and compliance in collaboration with senior RA leadership, Supply Chain, Distribution, and other stakeholders, ensuring all critical timelines are met.
Post-Doctoral Regulatory Affairs Fellow - Advertising and Promotion Boehringer Ingelheim International GmbHPost-Doctoral Regulatory Affairs Fellow - Advertising and PromotionRidgefield, CTThe Regulatory Affairs Fellow - Advertising and Promotion is a post-doctoral pharmacist position that will obtain broad exposure to BI US Medical functions including, but not limited to -- Medical Affairs and Scientific Communications, clinical operations, translational medicine and clinical pharmacology, and regulatory affairs. The Fellow will be based at Boehringer Ingelheim´s U.S. headquarters in Ridgefield, CT, working on a particular or multiple therapeutic areas (TAs) in the areas of cardiology, diabetes, immunology, oncology, and respiratory.
Postdoctoral Regulatory Affairs Fellow - Product Labeling Content Boehringer Ingelheim International GmbHPostdoctoral Regulatory Affairs Fellow - Product Labeling ContentRidgefield, CTSupport late-stage development labeling for NCEs/NBEs and labeling supplements initiated by BI, in conjunction with RA Product Labeling Management and the assigned RA Product Manager in the RA Product Groups. The Fellow will be based at Boehringer Ingelheim´s U.S. headquarters in Ridgefield, CT, working on a particular or multiple therapeutic areas (TAs) in the areas of cardiology, diabetes, immunology, oncology, and respiratory.
Postdoctoral Regulatory Affairs Fellow - Product Strategy Boehringer Ingelheim International GmbHPostdoctoral Regulatory Affairs Fellow - Product StrategyRidgefield, CTWith supervision, the Product Group Regulatory Affairs Fellow will: Regulatory Professionalism: As a regulatory professional with basic knowledge in one or more therapeutic areas, interact effectively at all levels of the organization (local and global), within Regulatory Affairs and across functions, as a US regulatory advocate to achieve common goals for assigned projects. RA Subteams and Intra-RA Project Responsibilities: Effectively contribute US operational and strategic perspectives to RA subteam to ensure GRL and the subteam accurately consider US regulatory requirements and challenges in the global context.
Postdoctoral Regulatory Affairs Fellow - Policy and Intelligence Boehringer Ingelheim International GmbHPostdoctoral Regulatory Affairs Fellow - Policy and IntelligenceRidgefield, CTThe Clinical Development and Medical Affairs Fellow is a post-doctoral pharmacist position that will obtain broad exposure to BI US Medical functions including, but not limited to -- Medical Affairs and Scientific Communications, clinical operations, translational medicine and clinical pharmacology, and regulatory affairs. With supervision, the Regulatory Policy and Intelligence Fellow will: Proactively review and evaluate relevant US regulations and guidelines, as well as evolving regulatory trends and developments for their impact on drug and device development activities and on existing development strategies.
Postdoctoral Fellow - Medical Affairs and Scientific Communication (PharmD) Boehringer Ingelheim International GmbHPostdoctoral Fellow - Medical Affairs and Scientific Communication (PharmD)Ridgefield, CTThe Fellow will be based at Boehringer Ingelheim´s U.S. headquarters in Ridgefield, CT, working on a particular or multiple therapeutic areas (TAs) in the areas of cardio-renal-metabolism, Mental Health, oncology, and respiratory. Scientific Communications: Review and provide medical and scientific expertise to ensure the accuracy, clarity, and compliance of promotional and non-promotional materials, including marketing materials, educational content, sales aids, and training materials.